About this trial

This is a prospective, multicenter study conducted within the Chinese Children's Cancer Group (CCCG). The study aims to evaluate whether the addition of three novel agents, dasatinib, venetoclax and homoharringtonine, can improve the minimal residual disease (MRD)-negative remission rate, enhance event-free survival (EFS), and reduce the cumulative incidence of relapse (CIR) in pediatric patients with newly diagnosed T-cell acute lymphoblastic leukemia (T-ALL).

Eligibility criteria

Qualifiers

Age older than 1 month to younger than 18 years.

Diagnosis of acute lymphoblastic leukemia by bone marrow morphology.

Diagnosis of T-ALL by immunophenotyping.

Disqualifiers

B-ALL

AML

Acute leukemias of ambiguous lineage diagnosed according to WHO or EGIL criteria.

ALL evolved from chronic myeloid leukemia (CML).

Trial design

Treatments tested in this trial

  • Venetoclax
  • Dasatinib
  • homoharringtonine

Treatment groups

610 Participants
are divided into 3 treatment groups

Locations

27
China
Anhui Medical University Second Affiliated Hospital HefeiAnhui, China
Anhui Provincial Children's Hospital HefeiAnhui, China
Chongqing Medical University Affiliated Children's Hospital ChongqingChongqing Municipality, China
Fujian Medical University Union Hospital FuzhouFujian, China

Sponsors and collaborators

Institute of Hematology & Blood Diseases Hospital, China

Lead sponsor